Detection of NDM-1, VIM-1, KPC, OXA-48, and OXA-162 carbapenemases by matrix-assisted laser desorption ionization-time of flight mass spectrometry
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Validation Study
PubMed
22553235
PubMed Central
PMC3405576
DOI
10.1128/jcm.01002-12
PII: JCM.01002-12
Knihovny.cz E-resources
- MeSH
- Acinetobacter baumannii enzymology MeSH
- Bacterial Proteins metabolism MeSH
- beta-Lactamases metabolism MeSH
- Enterobacteriaceae enzymology MeSH
- Enterobacteriaceae Infections microbiology MeSH
- Hydrolysis MeSH
- Humans MeSH
- Meropenem MeSH
- Microbial Sensitivity Tests methods MeSH
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization methods MeSH
- Thienamycins metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Validation Study MeSH
- Names of Substances
- Bacterial Proteins MeSH
- beta-Lactamases MeSH
- carbapenemase MeSH Browser
- Meropenem MeSH
- Thienamycins MeSH
Matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) is a potentially useful tool for the detection of antimicrobial resistance, especially that conferred by β-lactamases. Here we describe a modification of a previously reported MALDI-TOF MS meropenem hydrolysis assay. The modified method was validated on 108 carbapenemase-producing members of the Enterobacteriaceae, two NDM-1-producing Acinetobacter baumannii isolates, and 35 carbapenem-resistant enterobacteria producing no carbapenemase. The detection of carbapenemases by MALDI-TOF MS seems to be a powerful, quick, and cost-effective method for microbiological laboratories.
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